Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Let the assistant find your predicates

Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: QNM FDA class 2

Mountable Electromechanical Surgical System For Transluminal Approaches

General, Plastic Surgery

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The Mountable Electromechanical Surgical System for Transluminal Approaches is a software-controlled, patient bed- and/or operating table-mounted electromechanical system with human/device interfaces that enables a qualified user to perform transluminal endoscopic or laparoscopic surgical procedures using surgical instruments attached to an electromechanical arm. This device is classified as FDA Class 2, requiring 510(k) clearance, under regulation 878.4961 in the General and Plastic Surgery specialty. It carries product code QNM and is not an implant and not life-sustaining.

510(k) Clearances

8 matches
K Number
Device Name
Anovo Surgical System (Model 6Ne); Anovo Instrument ARM Curved Scissors ; Anovo Instrument ARM Hook Electrode
Anovo Surgical System (6Ne)
Anovo Instrument ARM Curved Scissors ; Anovo Instrument ARM Hook Electrode
Anovo Instrument ARM Curved Scissors; Anovo Instrument ARM Hook Electrode
Anovo Surgical System (Model 6Ne)
Anovo Surgical System (model 6N)
Anovo Pedestal
Hominis Surgical System

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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